Understanding G6PD Deficiency in Newborns and the Importance of Universal Newborn Screening: A Closer Look at Trivitron's Neonatal G6PD Kit
G6PD deficiency is a genetic condition that affects the functioning of red blood cells. It is caused by a mutation in the G6PD gene, which is located on the X chromosome. Due to the fact that males have only one X chromosome, they are more likely to develop G6PD deficiency than females. G6PD Deficiency in Newborns can experience episodes of hemolysis, which is the destruction of red blood...
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